Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15260 | A10 | 15678972 | C | T | missense_variant | MODERATE | c.2752G>A|p.Ala918Thr |
S140 |
2 | BAA10g15260 | A10 | 15679081 | G | A | synonymous_variant | LOW | c.2643C>T|p.Leu881Leu |
S112 |
3 | BAA10g15260 | A10 | 15679770 | G | A | missense_variant&splice_region_variant | MODERATE | c.2224C>T|p.Pro742Ser |
S120 |
4 | BAA10g15260 | A10 | 15680091 | C | T | splice_region_variant&intron_variant | LOW | c.1983+5G>A| |
S25 |
5 | BAA10g15260 | A10 | 15680288 | C | T | synonymous_variant | LOW | c.1878G>A|p.Glu626Glu |
S144 |
6 | BAA10g15260 | A10 | 15681760 | C | T | missense_variant | MODERATE | c.590G>A|p.Gly197Glu |
S117 |
7 | BAA10g15260 | A10 | 15682045 | C | T | missense_variant | MODERATE | c.373G>A|p.Ala125Thr |
S277 |
8 | BAA10g15260 | A10 | 15682338 | C | T | missense_variant | MODERATE | c.163G>A|p.Glu55Lys |
S33 |
9 | BAA10g15260 | A10 | 15683431 | C | T | missense_variant | MODERATE | c.40G>A|p.Glu14Lys |
S189 |
10 | BAA10g15260 | A10 | 15684217 | C | T | upstream_gene_variant | MODIFIER | c.-747G>A| |
S211 S227 |
11 | BAA10g15260 | A10 | 15686711 | C | T | upstream_gene_variant | MODIFIER | c.-3241G>A| |
S249 |
12 | BAA10g15260 | A10 | 15686774 | G | A | upstream_gene_variant | MODIFIER | c.-3304C>T| |
S216 S241 S265 |